Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5743618 | 0.677 | 0.360 | 4 | 38797027 | missense variant | C/A | snv | 0.53 | 0.51 | 6 | |
rs7936323 | 0.882 | 0.160 | 11 | 76582714 | intergenic variant | G/A | snv | 0.44 | 6 | ||
rs2428494 | 0.827 | 0.160 | 6 | 31354420 | intron variant | T/A;C | snv | 5 | |||
rs1438673 | 0.882 | 0.120 | 5 | 111131801 | downstream gene variant | C/T | snv | 0.61 | 4 | ||
rs17294280 | 0.882 | 0.120 | 15 | 67175947 | intron variant | A/G | snv | 0.19 | 4 | ||
rs10519067 | 0.925 | 0.120 | 15 | 60776148 | intron variant | G/A | snv | 0.20 | 3 | ||
rs9775039 | 0.925 | 0.120 | 9 | 6177453 | intergenic variant | G/A | snv | 0.20 | 3 | ||
rs1523643 | 0.925 | 0.120 | 8 | 16931726 | intergenic variant | G/A;T | snv | 2 |